Evidence map›Paper›PMID 40495676›Full record

ArticleDevelopment (Cambridge, England)2025

Migration of Kupffer's vesicle-derived cells is essential for tail morphogenesis in zebrafish embryos.

Jelmer Hoeksma, Jeroen den Hertog

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Jelmer HoeksmaHubrecht Institute - KNAW and University Medical Center Utrecht, Utrecht, The Netherlands.
Jeroen den HertogHubrecht Institute - KNAW and University Medical Center Utrecht, Utrecht, The Netherlands.ORCID 0000-0002-8642-8088

Funding

Leiden University
6 · The paper itself

Abstract

A phenotypic screen of fungal filtrates on developing zebrafish embryos identified metabolites from the fungus Ceratocystis populicola to induce ectopic tail formation, including a split notochord and a duplicated caudal fin. Chemical analyses led to the identification of monoterpene alcohols, in particular geraniol, as the active compounds. Tüpfel long fin zebrafish embryos were more susceptible to geraniol-induced ectopic tail formation than Wild Indian Karyotpe zebrafish embryos. RNA-sequencing on tail buds of 15-somite-stage embryos revealed downregulation of essential genes of the retinoic acid signaling pathway. Differential expression of cyp26a1, fgf8a and downstream hox-genes was validated. Time-lapse imaging revealed that Kupffer's vesicle-derived cells failed to migrate after Kupffer's vesicle collapse upon geraniol treatment. These cells failed to merge with progenitors from the tail bud and contributed to an ectopic tail, expressing markers for presomitic mesoderm, somite and notochord tissue. Strikingly, ablation of Kupffer's vesicle by tbxta-morpholino injection rescued ectopic tail formation. Taken together, our data suggest that Kupffer's vesicle cells harbor tail progenitor capacity, and proper migration of these cells is essential for normal tail morphogenesis.

Indexed as

Cell MovementMorphogenesisTailZebrafishAnimalsEmbryo, NonmammalianFibroblast Growth FactorsGene Expression Regulation, DevelopmentalNotochordRetinoic Acid 4-HydroxylaseSignal TransductionZebrafish Proteinscyp26a1 protein, zebrafishfgf8a protein, zebrafishFibroblast Growth FactorsRetinoic Acid 4-HydroxylaseZebrafish ProteinsGeraniolKupffer's vesicleTail morphogenesisZebrafish

Identifiers

PMID40495676
PMCPMC12211557

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.